Canonical Allele Identifier: CA963329359

Gene: GCH1

Linked Data

• dbSNP Id: rs2039615039
• gnomAD v3: 14-54844830-A-G
• gnomAD v4: 14-54844830-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.54844830A>G , CM000676.2:g.54844830A>G	GRCh38
NC_000014.8:g.55311548A>G , CM000676.1:g.55311548A>G	GRCh37
NC_000014.7:g.54381298A>G	NCBI36
NG_008647.1:g.62995T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000491895.7:c.627-687T>C MANE Select	ENSP00000419045.2:n.627-687T>C
ENST00000254299.8:n.775-687T>C
ENST00000395514.5:c.627-687T>C	ENSP00000378890.1:n.627-687T>C
ENST00000395521.6:n.293-1776T>C
ENST00000491895.6:c.627-687T>C	ENSP00000419045.2:n.627-687T>C
ENST00000536224.2:c.626+938T>C	ENSP00000445246.2:n.626+938T>C
ENST00000543643.6:c.626+938T>C	ENSP00000444011.2:n.626+938T>C
ENST00000622544.4:c.627-687T>C	ENSP00000477796.1:n.627-687T>C
NM_000161.2:c.627-687T>C	NP_000152.1:n.627-687T>C
NM_001024024.1:c.627-687T>C	NP_001019195.1:n.627-687T>C
NM_001024070.1:c.626+938T>C	NP_001019241.1:n.626+938T>C
NM_001024071.1:c.626+938T>C	NP_001019242.1:n.626+938T>C
XM_005267530.1:c.626+938T>C	XP_005267587.1:n.626+938T>C
XM_017021218.1:c.333-687T>C	XP_016876707.1:n.333-687T>C
NM_000161.3:c.627-687T>C MANE Select	NP_000152.1:n.627-687T>C
NM_001024070.2:c.626+938T>C	NP_001019241.1:n.626+938T>C
NM_001024071.2:c.626+938T>C	NP_001019242.1:n.626+938T>C
NM_001024024.2:c.627-687T>C	NP_001019195.1:n.627-687T>C